Evidence map›Paper›PMID 35011660›Full record

ArticleCells2021

Association between Exosomal miRNAs and Coronary Artery Disease by Next-Generation Sequencing.

Sheng-Nan Chang, Jien-Jiun Chen, Jo-Hsuan Wu, Yao-Te Chung, Jin-Wun Chen, Chu-Hsuan Chiu, Chia-Ju Liu, Meng-Tsun Liu, Yi-Cheng Chang, Chin Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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  16. Autophagy and autophagy-related pathways in cancer.Nature reviews. Molecular cell biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Sheng-Nan ChangDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.ORCID 0000-0002-2663-5042
Jien-Jiun ChenDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.
Jo-Hsuan WuShiley Eye Institute and Viterbi Family Department of Ophthalmology, University of California, San Diego, CA 92093, USA.ORCID 0000-0002-9435-746X
Yao-Te ChungDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.
Jin-Wun ChenDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.
Chu-Hsuan ChiuGraduate Institute of Medical Genomics and Proteomics, National Taiwan University, Taipei 100, Taiwan.
Chia-Ju LiuDepartment of Nuclear Medicine, National Taiwan University Hospital, Taipei 100, Taiwan.ORCID 0000-0003-1641-5617
Meng-Tsun LiuDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.
Yi-Cheng ChangGraduate Institute of Medical Genomics and Proteomics, National Taiwan University, Taipei 100, Taiwan.ORCID 0000-0002-8077-5011
Chin LiDepartment of Biomedical Sciences, National Chung-Cheng University, Chia-Yi 62102, Taiwan.ORCID 0000-0002-5457-9623
Jou-Wei LinDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.ORCID 0000-0002-6110-7149
Juey-Jen HwangDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital Yunlin Branch, Douliu City 640203, Taiwan.
Wen-Pin LienDepartment of Internal Medicine, National Taiwan University Hospital, Taipei 100, Taiwan.
National Taiwan University Hospital · TWNational Taiwan University · TWNational Chung Cheng University · TWUniversity of California San Diego · US

Funding

National Taiwan University Hospital NTUHYL107.X005 and 110.X004
6 · The paper itself

Abstract

backgroundAmong various bio-informative molecules transferred by exosomes between cells, micro RNAs (miRNAs), which remain remarkably stable even after freeze-and-thaw cycles, are excellent candidates for potential biomarkers for coronary artery disease (CAD).

methodsBlood samples were collected from the coronary arteries of 214 patients diagnosed with three-vessel CAD and 140 without CAD. After precipitation extraction, the amounts of exosomes were found to decrease with increased age and three-vessel CAD. Next-generation sequencing was performed to further explore the possible relationship between exosomal miRNAs and CAD.

resultsEight exosomal miRNAs showed altered expression associated with CAD. The up-regulated miRNAs in CAD were miRNA-382-3p, miRNA-432-5p, miRNA-200a-3p, and miRNA-3613-3p. The down-regulated miRNAs were miRNA-125a-5p, miRNA-185-5p, miRNA-151a-3p, and miRNA-328-3p.

conclusionWe successfully demonstrated particular exosomal miRNAs that may serve as future biomarkers for CAD.

Indexed as

High-Throughput Nucleotide SequencingAgedCoronary Artery DiseaseExosomesFemaleHumansLinear ModelsMaleMicroRNAsMiddle AgedMicroRNAscoronary artery diseaseexosomesmicro RNAsnext-generation sequencing

Identifiers

PMID35011660
PMCPMC8750494
OpenAlexW4200157297

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.